Atypical antipsychotic agents having low affinity for the D2 Receptor

ABSTRACT

The present invention provides novel compounds of Formula I:  
                 
 
     The invention further relates to pharmaceutical compositions comprising compounds of Formula I and to methods of using compounds of Formula I to treat neuropsychiatric disorders (e.g., psychosis, depression, schizophrenia).

CROSS-REFERENCE TO RELATED APPLICATION

[0001] This application claims priority to U.S. Provisional Patent Application Serial No. 60/300,430, filed Jun. 26, 2001, which is hereby incorporated by reference in its entirety.

FIELD OF THE INVENTION

[0002] This invention relates to novel compounds and their use as antipsychotics. In particular, the invention relates to compounds having a typical dopamine receptor affinity, methods of preparing such compounds and to their use for therapeutic and drug screening purposes.

BACKGROUND OF THE INVENTION

[0003] There are currently several antipsychotics available for regular clinical use. Every one of them blocks dopamine D₂ receptors (Seeman and Tallerico 1998). See Index of Articles cited herein. This includes the older “typical” as well as the newer “a typical” antipsychotics. “Atypical” antipsychotic is a term that is used to define antipsychotics which have a lower or minimal incidence of side effects. With the exception of a few dopamine-depleting agents, there is no receptor-drug profile other than D₂ receptor blockage that is able to achieve antipsychotic activity. However, a central problem in the use of antipsychotics is that of related side effects. The two major side effects of concern have been extrapyramidal side effects (“EPS”) as well as prolactin elevation. Side effects limit the number of patients who agree to take these medications, as they tend to decrease compliance and high levels of EPS may actually decrease the efficacy of the medications.

[0004] Without being bound by theory, it is believed that EPS and prolactin elevation also result from dopamine D₂ blockade. In particular, the blockade of D₂ receptors in the tubero-infundibular system is thought to be responsible for prolactin elevation (Moore 1987), while the blockade of the dopamine D₂ receptors in the striatum is thought to be responsible for EPS (Farde et al. 1997). A corollary of prolonged blockade of the dopamine D₂ system is thought to be tardive dyskinesia which occurs after several years of use of antipsychotics that cause EPS (Casey 1996). Thus, avoiding these side effects is a central way of improving antipsychotics.

[0005] The current gold-standard for an a typical antipsychotic is clozapine. However, in some patients clozapine has the serious shortcoming of blood dyscrasias, or agranulocytosis, which means that all patients on this medication must have their blood tested regularly. This side-effect is the Achille's heel of clozapine. It has limited the use of this most effective antipsychotic (in terms of efficacy and “a typicality”) to being the drug of last resort because of this ongoing need for regular blood testing of each patient on the medication.

[0006] There is therefore a need for new effective antipsychotic drugs exhibiting minimal side effects (e.g., diminished or absent EPS, prolactin elevation and/or agranulocytosis side effects).

SUMMARY OF THE INVENTION

[0007] Novel tricyclic piperazine compounds have been prepared and found to have a high K_(i) (Note: K_(i)=K_(off)/K_(on)) for the dopamime D₂ receptor of at least 30 nM, preferably above about 40 nM, and/or a K_(off) sufficiently large to enable interaction between the dopamine D₂ receptor and the novel compound(s) to yield their beneficial “a typical” antipsychotic efficacy i.e., with greatly diminished or without the side effects associated with the “typical” antipsychotics. These compounds have been shown to act as a typical antipsychotics in animal behavior assays.

[0008] The present invention therefore provides compounds of Formula I:

[0009] wherein:

[0010] R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano, CH₃ and CH₃O;

[0011] R² is selected from the group consisting of C₂₋₅alkyl and (CH₂)_(n)OH;

[0012] X is selected from the group consisting of O and S;

[0013] n is 2-5; and

[0014] pharmaceutically acceptable salts, hydrates, prodrugs and solvates thereof.

[0015] According to other embodiments of the present invention, the above compounds of Formula I have a K_(i) value (affinity for the dopamine D₂ receptor) as noted below in items (1) to (12). Also, the below-noted K_(i) values are measured according to the procedures described in Seeman 1993 (cited herein) using raclopride as the standard ligand:

[0016] (1) K_(i) value for the dopamine D₂ receptor of at least 30 nM (nanomoles);

[0017] (2) K_(i) value for the dopamine D₂ receptor from 30 nM to about 500 nM;

[0018] (3) K_(i) value for the dopamine D₂ receptor of at least about 40 nM;

[0019] (4) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 50 nM;

[0020] (5) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 250 nM;

[0021] (6) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 180 nM;

[0022] (7) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 120 nM;

[0023] (8) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 80 nM;

[0024] (9) K_(i) value for the dopamine D₂ receptor of at least about ½×(K_(i) for clozapine);

[0025] (10) K_(i) value for the dopamine D₂ receptor from about ½×(K_(i) for clozapine) to about ½×(K_(i) for clozapine);

[0026] (11) K_(i) value for the dopamine D₂ receptor from about ½×(K_(i) for clozapine) to about 4×(K_(i) for clozapine); and

[0027] (12) K_(i) value for the dopamine D₂ receptor from about ½×(K_(i) for clozapine) to about 2×(K_(i) for clozapine).

[0028] The present invention also provides compounds of Formula I wherein R¹ is selected from the group consisting of halo and CF₃ and wherein R², X and n are as defined in Formula I.

[0029] The present invention also provides compounds of Formula I wherein R¹ is selected from the group consisting of F, Cl and CF₃, and wherein R², X and n are as defined in Formula I.

[0030] Further, the present invention provides compounds of Formula I wherein R¹ is Cl and wherein R², X and n are as defined in Formula I.

[0031] There are also provided compounds of Formula I wherein R¹ is selected from the group consisting of C₂₋₄ alkyl and (CH₂)_(n)OH and wherein R¹, X and n are as defined in Formula I. Further, the present invention provides compounds of Formula I wherein R² is selected from the group consisting of ethyl, n-propyl, isopropyl, butyl and (CH₂)₂OH and wherein R¹ and X are as defined in Formula I. The present invention further provides compounds of Formula I wherein R² is selected from the group consisting of ethyl and (CH₂)₂OH and wherein R¹ and X are as defined in Formula I.

[0032] There are also provided compounds of Formula I wherein X is O and wherein R², R¹ and n are as defined in Formula I.

[0033] The invention further relates to pharmaceutical compositions comprising a compound of Formula I and a pharmaceutically acceptable carrier and/or diluent.

[0034] According to another broad aspect of the present invention, there is provided a method of treating neuropsychiatric disorders (including, but not limited to, conditions associated with or leading to psychosis, emotional and behavioral disturbances, schizophrenia and schizophrenia spectrum disorders, psychotic disorders in the context of affective disorders, depression, psychosis disorders induced by drugs/medication (such as Parkinson's psychosis), drug induced movement disorders (dyskinesias in Parkinson's disease), psychosis and behavioral disorders in the context of dementias and psychotic disorders due to a general medical conditions, or combinations thereof) comprising administering to a patient or subject (e.g., a human or an animal such as a dog) in need thereof a therapeutically effectively amount of a compound of Formula I. Preferably, the compound of Formula I is combined with a pharmaceutically acceptable carrier and/or diluent.

[0035] Other features and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples while indicating preferred embodiments of the invention are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.

DETAILED DESCRIPTION OF THE INVENTION

[0036] 1. Definitions

[0037] The term “halo” as used herein means halogen and includes chloro, fluoro, bromo, and iodo.

[0038] The term “C₂₋₅alkyl” as used herein means straight and branched chain alkyl radicals containing from two to five carbon atoms and includes ethyl, propyl, isopropyl, n-butyl, t-butyl, n-pentyl and the like.

[0039] The term “compound(s) of the invention” as used herein means a compound of Formula I and salts, hydrates, prodrugs and solvates thereof.

[0040] The term “pharmaceutically acceptable salt” means an acid addition salt which is suitable for or compatible with the treatment of a patient or a subject such as a human patient or an animal such as a dog.

[0041] The term “pharmaceutically acceptable acid addition salt” as used herein means any non-toxic organic or inorganic salt of any base compounds represented by Formula I or any of their intermediates. Illustrative inorganic acids which form suitable acid addition salts include hydrochloric, hydrobromic, sulfuric and phosphoric acids, as well as metal salts such as sodium monohydrogen orthophosphate and potassium hydrogen sulfate. Illustrative organic acids that form suitable acid addition salts include mono-, di-, and tricarboxylic acids such as glycolic, lactic, pyruvic, malonic, succinic, glutaric, fumaric, malic, tartaric, citric, ascorbic, maleic, benzoic, phenylacetic, cinnamic and salicylic acids, as well as sulfonic acids such as p-toluene sulfonic and methanesulfonic acids. Either the mono or di-acid salts can be formed, and such salts may exist in either a hydrated, solvated or substantially anhydrous form. In general, the acid addition salts of compounds of Formula I are more soluble in water and various hydrophilic organic solvents, and generally demonstrate higher melting points in comparison to their free base forms. The selection of the appropriate salt will be known to one skilled in the art. Other non-pharmaceutically acceptable salts, e.g. oxalates, may be used, for example, in the isolation of compounds of Formula I for laboratory use, or for subsequent conversion to a pharmaceutically acceptable acid addition salt.

[0042] The term “solvate” as used herein means a compound of Formula 1, or a pharmaceutically acceptable salt of a compound of Formula I, wherein molecules of a suitable solvent are incorporated in the crystal lattice. A suitable solvent is physiologically tolerable at the dosage administered. Examples of suitable solvents are ethanol, water and the like. When water is the solvent, the molecule is referred to as a “hydrate.”

[0043] The term an “effective amount” or a “sufficient amount” of an agent as used herein is that amount sufficient to effect beneficial or desired results, including clinical results, and, as such, an “effective amount” depends upon the context in which it is being applied. For example, in the context of administering an agent that acts as an a typical antipsychotic, an effective amount of an agent is, for example, an amount sufficient to achieve such a reduction in psychoses, without unwanted side effects such as, for example EPS and prolactin elevation, as compared to the response obtained without administration of the agent. The term “effective amount” also includes that amount of the compound of Formula I which is “therapeutically effective” and which avoids or substantially attenuates undesirable side effects such as EPS, prolactin elevation and /or blood dyscrasias.

[0044] As used herein, and as well understood in the art, “treatment” is an approach for obtaining beneficial or desired results, including clinical results. Beneficial or desired clinical results can include, but are not limited to, alleviation or amelioration of one or more symptoms or conditions, diminishment of extent of disease, stabilized (i.e. not worsening) state of disease, preventing spread of disease, delay or slowing of disease progression, amelioration or palliation of the disease state, and remission (whether partial or total), whether detectable or undetectable. “Treatment” can also mean prolonging survival as compared to expected survival if not receiving treatment.

[0045] “Palliating” a disease or disorder means that the extent and/or undesirable clinical manifestations of a disorder or a disease state are lessened and/or time course of the progression is slowed or lengthened, as compared to not treating the disorder.

[0046] To “diminish” or “inhibit” or “suppress” or “reduce” a function or activity, such as psychoses, is to reduce the function or activity when compared to otherwise same conditions except for a condition or parameter of interest, or alternatively, as compared to another condition.

[0047] The terms “animal,” “subject” and “patient” as used herein include all members of the animal kingdom including, but not limited to, mammals, animals (e.g. cats, dogs, horses, etc.) and humans. The animal is preferably a human.

[0048] As used herein “low binding affinity” means a relatively high K_(i), of at least 30 nM (or at least about 40 nM), or of at least about ½×(K_(i) for clozapine) sufficient to yield the beneficial antipsychotic effects associated with “a typical” antipsychotics with reduced or diminished or altogether without the detrimental side effects of “typical” antipsychotics such as EPS etc. described above. The “low binding affinity” may be one that falls within ranges of items (1) to (12) noted above measured using raclopride as the standard ligand. As will be appreciated by those skilled in the art, K_(i) values depend on the method of measurement, pH, radiolabeling technique, tissue type, temperature and type of wash used. The greatest differences depend upon the ligand standard used, for example with clozapine, a K_(i) of 76 nM is obtained with raclopride as the standard, but a K_(i) of 180 nM is obtained when spiperone is used as the standard, even under identical conditions. Accordingly, K_(i) and “low binding affinity” as used herein encompass this understanding and the K_(i) values recited herein are based on K_(i) values measured using raclopride as the standard according to the procedure outlined in Seeman 1993. Preferably, a control K_(i) measurement should be made simultaneously, for example, with clozapine to standardize the K_(i) value measured to offset any effects of variations in the measuring conditions such as pH, temperature, tissue type etc. noted above.

[0049] As used herein a “fast off-rate” means a relatively high K_(off), on the order of approximately 0.6 min⁻¹ or greater sufficient to yield the beneficial antipsychotic effects associated with “a typical” antipsychotics with reduced or diminished or altogether without the detrimental side effects of “typical” antipsychotics such as EPS etc. described above. The same consideration in respect of K_(i) and low binding affinity also apply to K_(off) and “fast off-rate”. Thus, the “fast off-rate” may be one that falls within ranges of items (1)-(12) noted above using clozapine as the standard. See Kapur and Seaman 2000a.

[0050] 2. Preferred Compounds of the Invention

[0051] As hereinbefore described, it is expected that a typical antipsychotic activity may be achieved with a drug that blocks the dopamine D₂ receptor with a high K_(i), preferably of at least 30 nM, and/or a fast off-rate (Koff), preferably greater than about 0.6 min⁻¹ sufficient to yield the beneficial antipsychotic effects associated with “a typical” antipsychotics with reduced or diminished or altogether without the detrimental side effects of “typical” antipsychotics such as EPS etc. described above. Exemplary K_(off) values suitable for use with the present invention include, but are not limited to, from about 0.6 min⁻¹ to about 10.0 min⁻¹, from about 0.8 min⁻¹ to about 10.0 min⁻¹, from about 0.9 min⁻¹ to about 9.0 min⁻¹, from about 1.0 min⁻¹ to about 8.0 min⁻¹, from about 1.1 min⁻¹ to about 7.0 min⁻¹, from about 1.2 min⁻¹ to about 6.0 min⁻¹, from about 1.5 min⁻¹ to about 5.0 min⁻¹, and from about 1.8 min⁻¹ to about 3.2 min⁻¹. The measurement for K_(off) may be made according to the procedure outlined in Kapur and Seeman 2000a.

[0052] As noted above, according to one embodiment, the invention relates to novel compounds that have a K_(i) for the D₂ receptor of at least 30 nM and/or a K_(off) greater than about 0.6 min⁻¹. It has been found, more particularly, that D₂-binding ligands having the tricyclic structure:

[0053] have a K_(i) of at least 30 nM and/or a K_(off) of at least about 0.6 min⁻¹ (sufficient to yield the beneficial antipsychotic effects associated with “a typical” antipsychotics with reduced or diminished or altogether without the detrimental side effects of “typical” antipsychotics such as EPS etc. described above), and therefore are effective as atypical antipsychotics, when the piperazine group is derivatized by a group designated R² as noted below. In accordance with one of its aspects, the present invention therefore provides compounds of Formula I:

[0054] R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano,

[0055] CH₃ and CH₃O;

[0056] R² is selected from the group consisting of C₂₋₅alkyl and (CH₂)_(n)OH;

[0057] X is selected from the group consisting of O and S;

[0058] n is 2-5; and

[0059] pharmaceutically acceptable salts, hydrates, prodrugs and solvates thereof.

[0060] In accordance with one of its embodiments, the present invention therefore provides compounds of Formula I:

[0061] R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano, CH₃ and CH₃O;

[0062] R¹ is selected from the group consisting of C₂₋₅alkyl and (CH₂)_(n)OH;

[0063] X is selected from the group consisting of O and S;

[0064] n is 2-5; and

[0065] a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof; and wherein:

[0066] said compound of Formula I has a K_(i) for the dopamine D₂ receptor in any one of the value ranges noted in items (1) to (12) as follows:

[0067] (1) K_(i) value for the dopamine D₂ receptor of at least 30 nM (nanomoles);

[0068] (2) K_(i) value for the dopamine D₂ receptor from 30 nM to about 500 nM;

[0069] (3) K_(i) value for the dopamine D₂ receptor of at least about 40 nM;

[0070] (4) K_(i) value or the dopamine D₂ receptor from about 40 nM to about 500 nM;

[0071] (5) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 250 nM;

[0072] (6) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 180 nM;

[0073] (7) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 120 nM;

[0074] (8) K_(i) value for the dopamine D₂ receptor from about 40 nM to about 80 nM;

[0075] (9) K_(i) value for the dopamine D₂ receptor of at least about ½×(K_(i) for clozapine);

[0076] (10) K_(i) value for the dopamine D₂ receptor from about ½×(K_(i) for clozapine) to about 6½×(K_(i) for clozapine);

[0077] (11) K_(i) value for the dopamine D₂ receptor from about ½×(K_(i) for clozapine) to about 4×(K_(i) for clozapine); and

[0078] (12) K_(i) value for the dopamine D₂ receptor from about ½×(K_(i) for clozapine) to about 2×(K_(i) for clozapine).

[0079] As previously noted, the above-noted K_(i) values are measured according to the procedure described in Seeman 1993 (cited herein) using raclopride as the standard ligand.

[0080] In embodiments of the invention, compounds of Formula I are those in which R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano, CH₃ and CH₃O. Preferably, R¹ is selected from the group consisting of halo and CF₃. In more preferred embodiments, R¹ is selected from the group consisting of F, Cl and CF₃. In the most preferred embodiment, R¹ is Cl.

[0081] Further embodiments of the invention include compounds of Formula I wherein R¹ is selected from the group consisting of C₂₋₅alkyl and (CH₂)_(n)OH, where n is 2, 3, 4 or 5. Preferred embodiments include compounds of Formula I where R² is selected from the group consisting of C₂₋₄ alkyl and (CH₂)_(n)OH and n is 2-3. More preferably, R² is selected from the group consisting of ethyl, n-propyl, isopropyl, butyl and (CH₂)₂OH. Most preferred are compounds of Formula I wherein R² is selected from the group consisting of ethyl and (CH₂)₂OH.

[0082] Compounds of Formula I further include those in which X is selected from O and S. The oxazepines and thiazepines are expected to have a reduced propensity for the hematological side-effect, agranulocytosis (Uetrecht et al. 1997). This particular side effect is responsible for the limited clinical use of clozapine. Preferred are compounds of Formula I where X is O.

[0083] In specific embodiments of the invention, the compounds of Formula I include:

[0084] (A-1) 8-Trifluoromethyl-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0085] (A-2) 8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0086] (A-3) 8-Trifluoromethyl-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0087] (A-3a) 8-Trifluoromethyl-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0088] (A-4) 8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0089] (A-4a) 8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0090] (A-5) 8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0091] (A-5a) 8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0092] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0093] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0094] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0095] (A-8) 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0096] (A-9) 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0097] (A-10) 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0098] (A-11) 8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0099] (A-12) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0100] (A-13) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0101] (A-14) 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0102] (A-14a) 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl;

[0103] (A-15) 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0104] (A-15a) 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl;

[0105] (A-16) 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b.f][1,4]thiazepine; and

[0106] (A-16a) 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b.f][1,4]thiazepine.HCl.

[0107] More specifically the compounds of Formula I include:

[0108] (A-1) 8-Trifluoromethyl-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0109] (A-2) 8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0110] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0111] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0112] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0113] (A-11) 8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0114] (A-12) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

[0115] (A-13) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.

[0116] Even more specifically, the compounds of Formula I include:

[0117] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0118] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0119] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0120] (A-12) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

[0121] (A-13) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.

[0122] Most specifically, the compounds of Formula I include:

[0123] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0124] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl; and

[0125] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.

[0126] 3. Methods of Preparing Compounds of Formula I

[0127] Compounds of Formula I may be prepared using processes analogous to those known in the art. The present invention therefore provides, in a further aspect, a process for the preparation of a compound of Formula I, or a salt, solvate or hydrate thereof, which comprises the step of coupling a reagent of Formula A with a reagent of Formula B, as shown in Scheme 1, wherein R¹ and R² and X are as defined in Formula 1. Reagents of Formula A may be prepared from the corresponding lactams 2 by, for example, reaction with phosphorus oxychloride in an inert solvent, such as toluene, in the presence of an organic base, such as a tertiary amine, preferably at refluxing temperatures. Reagents A need not be isolated, but instead may be reacted directly with reagents of Formula B in an inert solvent such as toluene, preferably at refluxing temperatures. Alternatively, Reagents of Formula 2 may be reacted with a reagent of Formula B in the presence of a Lewis Acid such as TiCl₄ or BF₃Et₂O to provide compounds of Formula I.

[0128] Lactams 2, where X=O, may be prepared according to the procedures described in Klunder (J. Med. Chem. 1992, 35:1887). Alternatively, lactams 2, where X is O or S, may be prepared as shown in Scheme 2. Appropriately 4-substituted nitrobenzenes 3, wherein Y is a suitable leaving group such as halo, preferably fluoro or chloro, may be condensed with either aldehyde or esters 4, wherein X is O or S, using, for example potassium fluoride on alumina and phase transfer catalysis or by treating reagents 4 with a strong base, such as sodium hydride or sodium hydroxide, followed by the addition of reagents 3. Reduction of the nitro group, for example by Raney nickel catalyzed reduction, followed by saponification of the ester or oxidation of the aldehyde gives, after acidification (if necessary), an intermediate amino acid 5 that may be cyclized to lactam 2 by refluxing in an inert solvent such as xylenes or hexanes.

[0129] Reagents of Formula B are either commercially available or may be prepared using known procedures. For example, suitably mono-protected piperazines may be reacted with a compound of the formula Y—C₂₋₅alkyl or Y—(CH₂)_(n)OP, where Y is a leaving group such as halo and P is a suitable protecting group, in the presence of a base in an inert solvent, followed by removal of the protecting groups.

[0130] In some cases the chemistries outlined above may have to be modified, for instance by use of protective groups, to prevent side reactions due to reactive groups, such as reactive groups attached as substituents. This may be achieved by means of conventional protecting groups, for example as described in “Protective Groups in Organic Chemistry” McOmie, J. F. W. Ed., Plenum Press, 1973 and in Greene, T. W. and Wuts, P. G. M., “Protective Groups in Organic Synthesis”, John Wiley & Sons, 1991.

[0131] The formation of a desired compound salt is achieved using standard techniques. For example, the neutral compound is treated with an acid in a suitable solvent and the formed salt is isolated by filtration, extraction or any other suitable method. The conversion of a given compound salt to a desired compound salt is achieved by applying standard techniques, in which an aqueous solution of the given salt is treated with a solution of base, e.g. sodium carbonate or sodium or potassium hydroxide, to liberate the free base which is then extracted into an appropriate solvent, such as ether. The free base is then separated from the aqueous portion, dried and treated with the requisite acid as described above to give the desired salt.

[0132] The formation of solvates of the compounds of the invention will vary depending on the compound and the solvate. In general, solvates are formed by dissolving the compound in the appropriate solvent and isolating the solvate by cooling or using an antisolvent. The solvate is typically dried or azeotroped under ambient conditions.

[0133] Prodrugs of the compounds of the invention may be conventional esters formed with available hydroxy, amino or carboxyl group. For example, when R² is (CH₂)_(n)OH in a compound of Formula I, it may be acylated using an activated acid in the presence of a base, and optionally, in inert solvent (e.g. an acid chloride in pyridine). Some common esters which have been utilized as prodrugs are phenyl esters, aliphatic (C₈-C₂₄) esters, acyloxymethyl esters, carbamates and amino acid esters.

[0134] A radiolabeled compound of the invention may be prepared using standard methods known in the art. For example, tritium may be incorporated into a compound of the invention using standard techniques, for example by hydrogenation of a suitable precursor to a compound of the invention using tritium gas and a catalyst. Alternatively, a compound of the invention containing radioactive iodo may be prepared from the corresponding trialkyltin (suitably trimethyltin) derivative using standard iodination conditions, such as [¹²⁵I] sodium iodide in the presence of chloramine-T in a suitable solvent, such as dimethylformamide. The trialkyltin compound may be prepared from the corresponding non-radioactive halo, suitably iodo, compound using standard palladium-catalyzed stannylation conditions, for example hexamethylditin in the presence of tetrakis(triphenylphosphine) palladium (0) in an inert solvent, such as dioxane, and at elevated temperatures, suitably 50-100° C.

[0135] 4. Pharmaceutical Compositions

[0136] The compounds of the invention are preferably formulated into pharmaceutical compositions for administration to human subjects in a biologically compatible form suitable for administration in vivo. Accordingly, in another aspect, the present invention provides a pharmaceutical composition comprising a compound of Formula I in admixture with a suitable diluent and/or carrier.

[0137] The compositions containing the compounds of the invention can be prepared by known methods for the preparation of pharmaceutically acceptable compositions which can be administered to subjects, such that an effective quantity of the active substance is combined in a mixture with a pharmaceutically acceptable vehicle. Suitable vehicles are described, for example, in Remington's Pharmaceutical Sciences (Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa., USA 1985 and each of its later editions published to date). On this basis, the compositions include, albeit not exclusively, solutions of the substances in association with one or more pharmaceutically acceptable vehicles and/or diluents, and are contained in buffered solutions with a suitable pH and are iso-osmotic with the physiological fluids.

[0138] In accordance with the methods of the invention, the described compounds or salts or solvates thereof may be administered to a patient in a variety of forms depending on the selected route of administration, as will be understood by those skilled in the art. The compositions of the invention may be administered orally or parenterally. Parenteral administration includes intravenous, intraperitoneal, subcutaneous, intramuscular, transepithelial, nasal, intrapulmonary, intrathecal, rectal and topical modes of administration. Parenteral administration may be by continuous infusion over a selected period of time.

[0139] A compound of the invention or a salt or solvate thereof may be orally administered, for example, with an inert diluent or with an assimilable edible carrier, or it may be enclosed in hard or soft shell gelatin capsules, or it may be compressed into tablets, or it may be incorporated directly with the food of the diet. For oral therapeutic administration, the compound of the invention may be incorporated with excipient and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like.

[0140] A compound of the invention may also be administered parenterally or intraperitoneally. Solutions of a compound of the invention as a free base or pharmacologically acceptable salt or solvate can be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, DMSO and mixtures thereof with or without alcohol, and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms. A person skilled in the art would know how to prepare suitable formulations. Conventional procedures and ingredients for the selection and preparation of suitable formulations are described, for example, in Remington's Pharmaceutical Sciences (1990-18th edition) and in The United States Pharmacopeia: The National Formulary (USP 24 NF19) published in 1999.

[0141] The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersion and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases the form must be sterile and must be fluid to the extent that easy syringability exists.

[0142] The compounds of the invention may be administered to an animal alone or in combination with pharmaceutically acceptable carriers and/or diluents, as noted above, the proportion of which is determined by the solubility and chemical nature of the compound, chosen route of administration and standard pharmaceutical practice.

[0143] Preferably, the composition is in unit dose form such as a tablet, capsule or ampoule. Suitable unit doses, i.e. therapeutically effective amounts, can be determined during clinical trials designed appropriately for each of the conditions for which administration of a chosen compound is indicated and will of course vary depending on the desired clinical endpoint. It is anticipated that dosage sizes appropriate for administering the compounds of the invention will be roughly equivalent to those used currently for clozapine. Accordingly, each dosage unit for oral administration may contain from about 1 mg to about 500 mg, preferably from about 5 mg to about 450 mg, more preferably from about 10 mg to about 400 mg, even more preferably from about 15 mg to about 350 mg and most preferably from about 20 mg to about 300 mg and will be administered in a frequency appropriate for initial and maintenance treatments. In particular, on a routine basis, compounds of Formula I, will need to be given in a high concentration, the concentration which would bring the occupancy into the same range as other psychotic drugs. However, in the body of the recipient things are dynamic, and in the face of dynamic fluxes of dopamine these drugs with a fast K_(off) lead to a faster approach to equilibrium as well as more competitive displacement by dopamine.

[0144] 5. Uses

[0145] The present invention provides a new range of treatments of patients with psychotic disorders, preferably dopamine-related neuropsychiatric disorders. Accordingly, the present invention provides a method of treating neuropsychiatric disorders (including, but not limited to, conditions associated with or leading to psychosis, emotional and behavioral disturbances, schizophrenia and schizophrenia spectrum disorders, psychotic disorders in the context of affective disorders, depression, psychosis disorders induced by drugs/medication (such as Parkinson's psychosis), drug induced movement disorders (dyskinesias in Parkinson's disease), psychosis and behavioral disorders in the context of dementias and psychotic disorders due to a general medical conditions, or combinations thereof), comprising administering to a subject in need thereof an effective amount of a compound of Formula I. Preferably, the subject is a human or an animal (e.g., a dog) and the compound of Formula I is combined with a pharmaceutically acceptable carrier and/or diluent to provide a dosage composition as described hereinabove.

[0146] While not wishing to be bound to any one theory, it is hypothesized that it is the low receptor occupancy of the D₂ receptor with a drug having a high K_(i) and/or fast K_(off), which explain the “a typicality” of the compounds of the present invention. Affinity (more precisely, K_(i)) is, by definition, the ratio of K_(off)/K_(on) (the rate at which the drug moves off of and on to the receptor). In theory, either a difference in K_(on) and/or a difference in K_(off) could lead to low affinity. To examine where K_(on) or K_(off) drives the differences in D₂ affinity between typical and a typical antipsychotics, the affinity, K_(on) and K_(off) were measured for a series of typical and a typical antipsychotics (Kapur and Seeman 2000a). Although affinity for the D₂ receptor varied nearly a thousand-fold, from 0.025 nM for nemonapride to 155 nm for quetiapine, 99% of the difference in affinity of the antipsychotics was driven by differences in their K_(off) at the D₂ receptor. Differences in Kn did not account for any significant differences in affinity. All antipsychotics (typical or a typical) attach to the D₂ receptor with a similar rate constant; they typically differ only in how fast they come off of the receptor. It is proposed that this relationship between fast K_(off) and low affinity is an important underlying molecular feature that explains why low affinity at the D₂ receptor leads to the a typical antipsychotic effect with diminished or without the “typical” antipsychotic side effect profile. This theory also explains why drugs like risperidone and olanzapine do not act as a typical as clozapine (since their K_(off) is not as fast). Furthermore, this hypothesis has the ability to explain one fact that no previous hypothesis can explain, why drugs like remoxipride and amisulpride, which are pure D₂/D₃ antagonists demonstrate features of a typical antipsychotics. However, there is a limit to how fast one would want K_(off). Water, theoretically, has one of the fastest K_(off) on the dopamine receptor. While it does not give rise to side-effects, it is also not efficacious. Since some element of D₂ occupancy is essential to obtain antipsychotic effect, there is an optimal value of K_(off) which maximizes response with minimal side-effects.

[0147] The compounds of Formula I are useful since they demonstrate characteristics of a typical antipsychotic drugs with diminished or without the typical side effect antipsychotic drug profile. The compounds of Formula I are expected to provide improved psychotic symptoms without EPS with secondary improvement in negative symptoms, mood and cognition. While not wishing to limit the full range of disorders in animals which will benefit, compounds of Formula I are expected to be useful in conditions associated with or leading to psychosis and emotional and behavioral disturbances, including but not limited to schizophrenia and schizophrenia spectrum disorders; psychotic disorders in the context of affective disorders such as depression; psychotic disorders induced by drugs/medications (such as Parkinson's psychosis); drug-induced movement disorders (dyskinesias in Parkinson's Disease); psychotic and behavioral disorders in the context of dementias; and psychotic disorders due to a general medical condition.

[0148] As herein before mentioned, the side effect of agranulocytosis has limited the use of clozapine, the most effective antipsychotic (in terms of efficacy and “a typicality”) to being the drug of last resort. The best of current evidence suggests that clozapine's agranulocytosis is linked to its reactive metabolites (Uetrecht 1996). Furthermore, studies suggest that if one uses the tricyclic structure with an oxygen (dibenzoxazepine) or sulphur bridge (dibenzothiazepine) instead of the nitrogen (dibenzazepines) these reactive metabolites can be avoided (Uetrecht et al. 1997). This is supported by evidence that drugs which are similar to clozapine but avoid the dibenzazepine, e.g. the dibenzoxazepines such as loxapine and amoxapine, have never been implicated in agranulocytosis despite many years of use in high doses (Jegouzo et al. 1999). The compounds of the present invention, being oxazepines and thiazepines, are not expected to have the agranulocytosis side effect.

[0149] As hereinbefore mentioned, the inventors have prepared novel compounds of Formula I. Accordingly, the present invention includes all uses of the compounds of the invention including their use in therapeutic methods and compositions as antipsychotics, their use in diagnostic assays and their use as research tools.

[0150] The present invention further includes the use of a compound of Formula I to treat neuropsychiatric disorders, preferably a psychosis, more preferably schizophrenia and schizophrenia spectrum disorders. The present invention further includes a use of a compound or a composition of the invention to prepare a medicament for use to treat neuropsychiatric disorders, preferably a psychosis, more preferably schizophrenia and schizophrenia spectrum disorders.

[0151] The compounds of the invention can be used alone or in combination with other agents that have antipsychotic activity or in combination with other types of treatment (which may or may not have antipsychotic activity) for psychotic disorders.

[0152] In a particular aspect of the present invention, the compounds of the invention may be used in combination with other therapies and therapeutics to treat schizophrenia and schizophrenia spectrum disorders.

[0153] In addition to the above-mentioned therapeutic uses, the compounds of the invention are also useful in diagnostic assays, screening assays and as research tools.

[0154] In a specific embodiment, the present invention provides a method of treating neuropsychiatric disorders, preferably a psychosis, more preferably schizophrenia and schizophrenia spectrum disorders, comprising administering to an animal in need thereof, a therapeutically effective amount of a compound selected from the group of compounds:

[0155] (A-1) 8-Trifluoromethyl-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0156] (A-2) 8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0157] (A-3) 8-Trifluoromethyl-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0158] (A-3a) 8-Trifluoromethyl-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0159] (A-4) 8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0160] (A-4a) 8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0161] (A-5) 8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0162] (A-5a) 8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0163] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0164] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0165] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0166] (A-8) 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0167] (A-9) 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0168] (A-10) 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0169] (A-11) 8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0170] (A-12) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0171] (A-13) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0172] (A-14) 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

[0173] (A-14a) 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl;

[0174] (A-15) 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl;

[0175] (A-15a) 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl;.

[0176] (A-16) 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

[0177] (A-16a) 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl.

[0178] More specifically the present invention provides a method of treating neuropsychiatric disorders, preferably a psychosis, more preferably schizophrenia and schizophrenia spectrum disorders, comprising administering to an animal in need thereof, a therapeutically effective amount of a compound selected from the group of compounds:

[0179] (A-1) 8-Trifluoromethyl-1-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0180] (A-2) 8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0181] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine,

[0182] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0183] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0184] (A-11) 8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0185] (A-12) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

[0186] (A-13) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.

[0187] Even more specifically, the present invention provides a method of treating neuropsychiatric disorders, preferably a psychosis, more preferably schizophrenia and schizophrenia spectrum disorders, comprising administering to an animal in need thereof, a therapeutically effective amount of a compound selected from the group of compounds:

[0188] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0189] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl;

[0190] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0191] (A-12) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

[0192] (A-13) 8-Chloro-1-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.

[0193] Most specifically, the present invention provides a method of treating neuropsychiatric disorders, preferably a psychosis, more preferably schizophrenia and schizophrenia spectrum disorders, comprising administering to an animal in need thereof, a therapeutically effective amount of a compound selected from the group of compounds:

[0194] (A-6) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

[0195] (A-6a) 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl; and

[0196] (A-7) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.

[0197] Preferably, the animal is a human and the compound is combined with a pharmaceutically acceptable carrier and/or diluent to provide a dosage composition as described hereinbefore.

[0198] The following non-limiting examples are illustrative of the present invention:

EXAMPLES Example 1. 8-Trifluoromethyl-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0199] 8-Trifluoromethyl-10H-dibenzo[b,f][1,4]oxazepine-11-one (2, X=O, R¹=CF₃) (2.0 g, 7.16 mmol), phosphorus oxychloride (5 mL, 53 mmol), N,N-dimethylaniline (1.0 ml) and toluene (25 mL) were combined and heated to reflux for 3 hours. The mixture was evaporated under vacuum to afford the imino chloride intermediate A, X=OR¹=CF₃). This was used in the next step without further purification. Toluene 25 (25 ml) was added followed by 5 ml (45 mmol) of 1-ethylpiperazine. This mixture was refluxed for 3 hours. After evaporation the residue was added to a saturated aqueous K₂CO₃, which was extracted with chloroform. The chloroform phase was dried over magnesium sulfate, filtered and the solvent removed to give a viscous liquid. This was purified by flash chromatography on silica gel, eluting with 9:1 hexane:ethyl acetate, then 1:1 hexane:ethyl acetate and finally 100% ethyl acetate. Recrystallization from n-heptane gave the product as yellow crystals, mp 76-77° C., ¹H NMR (300 MHz, CDCl₃) δ1.16 (t, 3H, J=7.2 Hz, CH₃), 2.55 (q, 2H, J=7.2 Hz, —CH₂—), 2.59 (broad s, 4H, —CH₂—), 3.65 (broad s, 4H, —CH₂—), 7.20-7.25 (m, 2H), 7.27-7.30 (m, 2H), 7.35-7.39 (dd, J=1.5 and 7.5 Hz, 1H), 7.43 (broad s, 1H), 7.46-7.52 (ddd, J=1.8, 7.2, 8.1 Hz, 1H), MS (EI) m/z 375 (M⁺, 4.2%), 304 (8.5), 303 (15.1), 292 (5.8), 291 (25.5), 263 (6.9), 262 (18.4), 84 (100), 70 (5.0). HRMS calcd for C₂₀H₂₀N₃OF₃ 375.1558, found 375.1557.

Example 2 8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0200] Prepared in the same manner as Example 1 with 1-(2′-hydroxyethyl)piperazine. mp 110-111° C., ¹H NMR (300 MHz, CDCl₃) δ1.59 (broad s, 1H, —OH), 2.61-2.65 (overlapping broad s and t, 6H), 3.62 (broad s, 4H, —CH2-), 3.67 (t, 2H, —CH₂OH), 7.20-7.25 (m, 2H), 7.27-7.30 (m, 2H), 7.35-7.39 (dd, J=1.5 and 7.5 Hz, 1H), 7.43 (broad s, 1H), 7.46-7.52 (ddd, J=1.8, 7.2, 8.1 Hz, 1H), MS (EI) m/z 391 (M⁺, 2.1%), 292(8.20), 291(34.0), 263(8.3), 262(22.4), 113(45.1), 101(13.0), 100(100), 70(11.5), 70(9.8). HRMS calcd for C₂₀H₂₀N₃O₂F₃ 391.1508, found 391.1489.

Example 3 8-Trifluoromethyl-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl

[0201] Prepared in the same manner as Example 1 using 1-propylpiperazine, except that the residue obtained after flash chromatography was dissolved in ethyl acetate and the HCl salt precipitated as a white solid by the addition of 1 M HCl in ether. Mp 110 (decomposes), ¹H NMR (300 MHz, DMSO-d⁶) δ0.90 (t, 3H, —CH3), 1.17 (m, 2H, —CH₂—), 3.02 (m, 6H, piperazine —CH₂— and propyl —CH₂), 3.51 (broad s, 4H, —CH₂), 7.35-7.5 (m, 5H, overlapping Ar—H), 7.57 (dd, 1H, J=1.5 Hz and 7.5 Hz), 7.69 (doublet of triplets, 1H, J=1.5 Hz and 8 Hz), 10.96 (s, 1H, N+H), MS (EI) m/z 389 (M⁺ for free base, 4.9%), 303 (13.0), 291 (15.9), 193 (9.3), 111 (64.4), 98 (100), 56 (21.7). HRMS calcd for C₂₁H₂₂N₃₀F₃ 389.1715, found 389.1713.

Example 4 8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl

[0202] Prepared following the procedure of Example 3 using 1-isopropylpiperazine and had a mp 270° C. (decomposes), ¹H NMR (300 MHz, DMSO-d⁶) δ1.20 (d, 6H, J=6.6 Hz), 3.20 (broad s, 4H, —CH₂—), 3.45 (overlapping broad s and multiplet, 5H, —CH and —CH₂—), 7.35-7.45 (m, 5H, overlapping Ar—H), 7.57 (dd, 1H, J=1.5 Hz and 7.5 Hz), 7.64 (doublet of triplets, 1H, J=1.5 Hz and 8 Hz), 10.8 (s, 1H, N+H), MS (EI) m/z 389 (M⁺ for free base, 10.4%), 303 (21.0), 291 (16.3), 193 (13.3), 125 (74.1), 111 (58.5), 98 (100), 56 (37.7). HRMS calcd for C₂₁H₂₂N₃OF₃ 389.1715, found 389.1715.

Example 5 8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl

[0203] Prepared following the procedure of Example 3 with 1-butylpiperazine and had a mp 240° C. (decomposes), ¹H NMR (300 MHz, DMSO-d⁶) δ0.91 (t, 3H, J=7.5 Hz, —CH₃), 1.31 (m, 2H, —CH₂), 1.65 (m, 2H, —CH₂), 3.10 (broad s, 4H, —CH₂), 3.4-3.5 (overlapping multiplets, 6H, piperazinyl —CH₂— and butyl N—CH₂), 7.35-7.45 (m, 5H, overlapping Ar—H), 7.51 (dd, 1H, J=1.5 Hz and 7.5 Hz), 7.63 (doublet of triplets, 1H, J=1.5 Hz and 8 Hz), 10.2 (s, 1H, N+H), MS (EI) m/z 403 (M+for free base, 6.3%), 303 (18.5), 291 (17.7), 193 (12.4), 125 (74.1), 112 (100), 70 (37.1), 56 (6.9). HRMS calcd for C₂₂H₂₄N₃OF₃ 403.1871, found 403.1858.

Example 6 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,F][1,4]oxazepine (1b) and 8-chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.HCl

[0204] 8-Chloro-10H-dibenzo[b,f][1,4]oxazepin-11-one (2, X=0, R¹=Cl) (6.0 g, 24.4 mmol), phosphorus oxychloride (20 mL, 212 mmol), N,N-dimethylaniline (3.0 ml) and toluene (100 mL) were combined and heated to reflux for 3 hours. After evaporation, the residue was dissolved in 50 mls of toluene, 21.7 ml (170 mmol) of 1-ethylpiperazine was added and the mixture was refluxed for 3 hours. After evaporation, the residue was added to saturated aqueous K₂CO₃, which was extracted with chloroform. The chloroform phase was dried over MgSO₄, and after filtration the chloroform was evaporated to give a viscous liquid which was purified by flash chromatography on silica gel (9:1 hexane:ethyl acetate, then 1:1 hexane:ethyl acetate and finally 100% ethyl acetate). The crude free base form of the product was a low melting solid that had ¹H NMR (300 MHz, CDCl₃) δ 1.13 (t, 3H, CH₃), 2.45-2.60 (broad m, 6H, piperazinyl CH₂ and ethyl CH₂), 3.65 (broad s, 4H, CH₂), 6.92 (dd, 1H, J=2.5 and 8.5 Hz), 7.08 (d, 1H, J=8.5 Hz), 7.14 (d, 1H, J=2.5 Hz), 7.22 (doublet of triplets, 1H, J=1.6 and 7.6 Hz), 7.25 (dd, 1H, 1.4 and 8.1 Hz), 7.36 (dd, 1H, J=1.9 and 7.7 Hz), 7.48 (ddd, 1H, J=1.9, 7.7, 8.1 Hz). The solid was converted to the HCl salt by dissolving in ethyl acetate and adding 1N HCl. This gave a white solid (3.8 g, 43%), mp. 280 (decomposes), ¹H NMR (300 MHz, DMSO-d⁶) δ 1.24 (t, 3H, —CH₃), 3.18 (q, 2H, CH₂), 3.2-3.3 (broad, 4H, piperazinyl CH₂), 3.6-3.7 (Broad, 4H, piperazinyl CH₂), 7.07-7.13 (2H, m, overlapping coupled pair), 7.26 (dd, 1H, J=0.9 and 8.0 Hz), 7.36 (doublet of triplets, 1H, J=1.5 and 8.2 Hz), 7.43 (dd, 1H, 1.2 and 8.1 Hz), 7.52 (dd, 1H, 1.8 and 8.4 Hz), 7.64 (ddd, 1H, J=1.8, 8.0 and 8.4 Hz), MS (EI) m/z 341 (M⁺ for free base, 14.9%), 269(15.3), 257(41.5), 228(6.8), 193(24.3), 97(85.4), 84(100), HRMS calcd for C₁₉H₂₀N₃OCl 341.1295, found 341.1297.

Example 7 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0205] This was prepared in the same manner as Example 6 using 1-(2′-hydroxyethylpiperazine). The free base obtained by flash chromatography was recrystallized from 10:1 hexane:ethyl acetate to give yellow crystals of mp 149-150° C., ¹H NMR (300 MHz, CDCl₃), δ 1.66 (s, 1H, OH), 2.65-2.75 (m, 6H, overlapping —CH₂— peaks), 3.62 (broad s, 4H, piperazinyl CH₂), 3.68 (t, 2H, J=5.4 Hz), 6.92 (dd, 1H, J=2.5 and 8.5 Hz), 7.04 (d, 1H, J=8.5 Hz), 7.12 (d, 1H, J=2.5 Hz), 7.20 (doublet of triplets, 1H, J=1.6 and 7.6 Hz), 7.24 (dd, 1H, 1.4 and 8.1 Hz), 7.34 (dd, 1H, J=1.9 and 7.7 Hz), 7.46 (ddd, 1H, J=1.9, 7.7, 8.1 Hz), MS (EI) m/z 357 (M⁺, 2.0%), 229(6.5), 228(21.6), 113(45.9), 101(10.7), 100(100), 70(10.1), 69(10.8), HRMS calcd for C₁₉H₂₀N₃O₂Cl 357.1244, found 357.1254.

Example 8 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0206] Prepared in the same manner as Example 7 with 1-propylpiperazine and had a mp 90-91° C., ¹H NMR (300 MHz, CDCl₃), δ 0.93 (t, 3H, J=7.7 Hz, CH₃), 1.58 (m, 2H, CH₂), 2.39, (t, 2H, CH₂N), 2.55-2.65 (broad s, 4H, piperazinyl CH₂), 3.55-3.65 (broad s, 4H, piperazinyl CH₂), 6.89 (dd, 1H, J=2.5 and 8.5 Hz), 7.03 (d, 1H, J=8.5 Hz), 7.12 (d, 1H, J=2.5 Hz), 7.21 (doublet of triplets, 1H, J=1.6 and 7.6 Hz), 7.24 (dd, 1H, 1.4 and 8.1 Hz), 7.33 (dd, 1H, J=1.9 and 7.7 Hz), 7.45 (ddd, 1H, J=1.9, 7.7, 8.1 Hz), MS (EI) m/z 355 (M+, 11.0%), 269(15.7), 257(32.1), 228(15.7), 193(21.5), 111(80.3), 98(100), HRMS calcd for C₂₀H₂₂N₃OCl 355.1451, found 355.1457.

Example 9 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0207] Prepared in the same manner as Example 7 with 1-isopropylpiperazine and had a mp 55-56° C., ¹H NMR (300 MHz, CDCl₃), δ 1.08 (d, 6H, J=6.6 Hz, CH₃), 2.55-2.65 (broad s, 4H, piperazinyl CH₂), 2.74 (septet, 1H, J=6.6 Hz, CH), 3.55-3.65 (broad s, 4H, piperazinyl CH₂), 6.89 (dd, 1H, J=2.5 and 8.5 Hz), 7.02 (d, 1H, J=8.5 Hz), 7.12 (d, 1H, J=2.5 Hz), 7.19 (doublet of triplets, 1H, J=1.6 and 7.6 Hz), 7.24 (dd, 1H, 1.4 and 8.1 Hz), 7.33 (dd, 1H, J=1.9 and 7.7 Hz), 7.44 (ddd, 1H, J=1.9, 7.7, 8.1 Hz), MS (EI) m/z 355 (M⁺, 7.8%), 269(15.7), 257 (17.0), 245(10.8), 228(11.8), 193(19.7), 111(61.0), 98(100), 56 (46.5), HRMS calcd for C₂₀H₂₂N₃OCl 355.1451, found 355.1470.

Example 10 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0208] Prepared in the same manner as Example 7 with 1-butylpiperazine and had a mp 97-98° C., ¹H NMR (300 MHz, CDCl₃), δ 0.93 (t, 3H, J=7.5 Hz, CH₃), 1.35 (sextet, 2H, CH₂), 1.46 (quintet, 2H, CH₂), 2.40 (t, 2H, NCH₂), 2.55-2.65 (broad s, 4H, piperazinyl CH₂),3.55-3.65 (broad s, 4H, piperazinyl CH₂), 6.89 (dd, 1H, J=2.5 and 8.5 Hz), 7.02 (d, 1H, J=8.5 Hz), 7.12 (d, 1H, J=2.5 Hz), 7.19 (doublet of triplets, 1H, J=1.6 and 7.6 Hz), 7.24 (dd, 1H, 1.4 and 8.1 Hz), 7.33 (dd, 1H, J=1.9 and 7.7 Hz), 7.44 (ddd, 1H, J=1.9, 7.7, 8.1 Hz), MS (EI) m/z 369 (M⁺, 8.7%), 291 (30.5), 269 (15.1), 257 (24.8), 228(13.8), 193(25.0), 125(78.9), 112(100), 70(40.9), HRMS calcd for C₂₁H₂₄N₃OCl 369.1608, found 369.1604.

Example 11 8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine

[0209] Prepared in the same manner as Example 1 starting with 8-fluoro-10H-dibenzo[b,f][1,4]oxazepin-11-one (2, X=O, R¹=F) with 1-ethyl piperazine. This compound was an oil with ¹H NMR (400 MHz, CDCl₃), 61.16 (t, 3H, J=7.2 Hz, CH₃), 2.55 (q, 2H, J=7.2 Hz, —CH₂—), 2.55-2.65 (broad s, 4H, piperazinyl CH₂), 3.55-3.65 (broad s, 4H, piperazinyl CH₂), 6.64 (ddd, 1H, J 2.4, 6.6 and 7.2 Hz), 6.82 (dd, 1H, J=2.1 and 7.5 Hz), 7.12 (dd, 1H, J=4.2 and 6.2 Hz), 7.21 (doublet of triplets, 1H, J=0.8 and 6.0 Hz), 7.23 (dd, 1H, J=0.9 and 6.3 Hz), 7.34 (dd, 1H, J=1.2 and 5.7 Hz), 7.44 (doublet of triplets, 1H, J=1.2 and 6.0 Hz).

Example 12. 8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine

[0210] 8-Chloro-10H-dibenzo[b,f][1,4]thiazepin-11-one 2 (X=S and R¹=Cl) (0.5 g, 1.91 mol), phosphorus oxychloride (5 ml, 53 mmol), toluene (25 ml) and N,N-dimethylaniline (1.0 ml) were heated at reflux for 3 hours. After evaporation of the volatiles, 25 ml of toluene and 5 ml (45 mmol) of 1-ethylpiperazine were added. Work-up and purification as described in Example 1 gave 150 mg (22%) of light yellow crystals, mp 100-101° C., ¹H NMR (300 MHz, CDCl₃), 81.11 (t, 3H, J=6.0 Hz, CH₃), 2.55 (q, 2H, J=6.0 Hz, —CH₂—), 2.55-2.65 (broad s, 4H, piperazinyl CH₂), 3.55-3.65 (broad s, 4H, piperazinyl CH₂), 6.83 (dd, 1H, J=1.5 and 6.0 Hz), 7.07 (d, 1H, J=1.5 Hz), 7.25-7.40 (mult., 4H), 7.50 (dd, 1H, J=7.5 Hz), MS (EI) m/z 357 (M⁺, 16.1%), 244(34.2), 209(30.1), 97(93.7), 84(100), HRMS calcd for C₁₉H₂₀N₃SCl 357.1066, found 357.1067.

Example 13 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine

[0211] Prepared following the procedure of Example 12 using 1-(2′-hydroxyethyl)piperazine and had mp 110-111° C., ¹H NMR (300 MHz, CDCl₃), δ 2.55-2.65 (broad s, 4H, piperazinyl CH₂), 2.64 (t, 2H, J=7.5 Hz, CH₂—), 3.55-3.65 (broad s, 4H, piperazinyl CH₂), 3.68 (t, 2H, J=7.5 Hz, —CH₃OH), 6.88 (dd, 1H, J=1.5 and 6.0 Hz), 7.11 (d, 1H, J=1.5 Hz), 7.30-7.40 (mult., 4H), 7.54 (dd, 1H, J=7.5 Hz), MS (EI) m/z 373 (M⁺, 6.1%), 244(53.9), 209(47.0), 113(42.0), 100(100), HRMS calcd for C₁₉H₂₀N₃₀SCl

Example 14 8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl

[0212] Prepared using the procedure of Example 12 using 1-propylpiperazine, the HCl salt being obtained by dissolving the residue obtained from flash chromatography in ethyl acetate and precipitating the salt with 1N HCl in ether. The salt was a hygroscopic white solid with ¹H NMR (300 MHz, DMSO-d⁶), δ 0.90 (t, 3H, CH₃), 1.70 (m, 2H, —CH₂—), 3.00 (t, 2H, —CH₂N), 3.0-3.1 (broad s, 4H, piperazinyl CH₂), 3.5-3.6 (broad s, 4H, piperazinyl CH₂), 7.00 (dd, 1H, J=2.1 and 8.4 Hz), 7.07 (d, 1H, J=2.1 Hz), 7.40 (d, 1H, J=8.4 Hz), 7.5-7.6 (m, 4H), 10.7 (s, 1H, N⁺H), MS (EI) m/z 371 (M⁺ for free base, 55.1%), 286(51.0), 244 (30.2), 209(23.6), 111 (19.1), 97(100), HRMS calcd for C₂₀H₂₂N₃SCl 371.1223, found 371.1233.

Example 15 8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl

[0213] Prepared using the procedure of Example 12 using 1-isopropylpiperazine, the HCl salt being obtained by dissolving the residue obtained from flash chromatography in ethyl acetate and precipitating the salt with 1N HCl in ether. The salt had a mp 140 (decomposes), 1¹H NMR (300 MHz, DMSO-d⁶), δ 1.31 (d, 6H, CH₃), 3.0-3.1 (broad s, 4H, piperazinyl CH₂), 3.3 (septet, 1H, CH), 3.5-3.6 (broad s, 4H, piperazinyl CH₂), 7.02 (dd, 1H, J=2.1 and 8.4 Hz), 7.11 (d, 1H, J=2.1 Hz), 7.43 (d, 11H, J=8.4 Hz), 7.5-7.6 (m, 4H), 11.0 (s, 1H, N⁺H), MS (EI) m/z 371 (M+for free base, 7.2%), 286(13.1), 244 (18.6), 209(25.7), 111 (66.8), 98(100), HRMS calcd for C₂₀H₂₂N₃SCl 371.1223, found 371.1234.

Example 16 8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.HCl

[0214] Prepared using the procedure of Example 12 using 1-butylpiperazine, the HCl salt being obtained by dissolving the residue obtained from flash chromatography in ethyl acetate and precipitating the salt with 1N HCl in ether. The salt was a hygroscopic white solid and ¹H NMR (300 MHz, DMSO-d⁶), δ 0.99 (t, 3H, CH₃), 1.33 (2H, m), 1.69 (2H, m), 3.02 (t, 2H, NCH₂, 3.1-3.2 (broad s, 4H, piperazinyl CH₂), 3.5-3.6 (broad s, 4H, piperazinyl CH₂), 7.02 (dd, 1H, J=2.1 and 8.4 Hz), 7.11 (d, 1H, J=2.1 Hz), 7.43 (d, 1H, J=8.4 Hz), 7.5-7.6 (m, 4H), 9.9 (s, 1H, N⁺H). TABLE 1 Summary of Examples for Compounds of Formula 1 I

Example # R¹ R² X 1 CF₃ CH₂CH₃ O 2 CF₃ CH₂CH₂OH O 3 CF₃ CH₂CH₂CH₃ O 4 CF₃ CH(CH₃)₂ O 5 CF₃ CH₂CH₂CH₂CH₃ O 6 Cl CH₂CH₃ O 7 Cl CH₂CH₂OH O 8 Cl CH₂CH₂CH₃ O 9 Cl CH(CH₃)₂ O 10 Cl CH₂CH₂CH₂CH₃ O 11 F CH₂CH₃ O 12 Cl CH₂CH₃ S 13 Cl CH₂CH₂OH S 14 Cl CH₂CH₂CH₃ S 15 Cl CH(CH₃)₂ S 16 Cl CH₂CH₂CH₂CH₃ S

Example 17 8-Trifluoromethyl-10H-dibenzo[b,f][1,4]oxazepin-11-one (Formula 2, X=O, R¹=CF₃)

[0215] (a) Methyl salicylate (30.4 g, 0.20 mol), 4-fluoro-3-nitrobenzotrifluoride (41.8 g, 0.20 mol), 18-crown-6 (10.6 g, 0.04 mol), 40% w.w potassium fluoride-alumina and acetonitrile (200 ml) were refluxed for 4 hours. After cooling, 500 mls each of water and diethyl ether were added, and the mixture was transferred to a separatory funnel. After vigorous mixing the aqueous layer and alumina sediments were discarded, and the organic phase was washed twice with 200 mls of saturated potassium chloride solution. The organic layer was dried over MgSO₄, and after filtration, the volatiles were removed by rotary evaporator to give 50.9 g (74.6% yield) of methyl O-(2-nitro-4-trifluoromethylphenyl)salicylate, mp 56-57° C., ¹H NMR (300 MHz, CDCl₃), δ 3.75 (s, 3H), 6.82 (d, 1H, J=8.7 Hz), 7.21 (d, 1H, J=8.7 Hz), 7.40 (t, 1H, J=7.8 Hz), 7.63-7.67 (m, 2H), 8.06 (dd, 1H, J=1.2 Hz, J=6.0 Hz), 8.25 (d, 1H, J=1.5 Hz).

[0216] (b) Methyl O-(2-nitro-4-trifluoromethylphenyl)salicylate (30.0 g, 0.088 mol) was dissolved in 150 ml of methanol and hydrogenated over Raney nickel (7.5 g) at room temperature and 50 psi pressure for 6 hours. After filtration to remove the catalyst, the methanol was removed and the residue dissolved in tetrahydrofuran (50 ml) and methanol (50 ml), followed by treatment with 5 N NaOH (20 ml) for 3 hours. After concentration in vacuo, the residue was acidified to pH 1-2 with 6 N HCl. The resulting suspension was filtered to give a solid which was recrystallized from n-heptane to provide O-(2-amino-4-trifluoromethylphenyl)salicylic acid as light gray solid, 13.3 g, 50.9%, mp 108-109.

[0217] (c) The aminosalicylic acid (17.3 g, 58.2 mmol) was refluxed in 150 ml of xylene for 24 hours with continuous removal of water. The xylene was removed, and the residue was recrystallized from methanol to provide 8-trifluoromethyl-10H-dibenzo[b,f][1,4]oxazepin-11-one as a white solid, mp 246-247° C., ¹H NMR (DMSO-d⁶), δ 7.38-7.66 (m, 7H), 10.7 (s, 1H, NH).

Example 18 8-Chloro-10H-dibenzo[b,f][1,4]oxazepin-11-one (Formula 2, X=O, R¹=Cl)

[0218] (a) Salicylaldehyde (0.386 mol) was dissolved in anhydrous DMF (300 ml), and allowed to react with 6.84 g of sodium hydride (95%, 0.27 mol). After the reaction was complete, 2,5-dichloronitrobenzene (40 g, 0.208 mol) was added all at once, and the reaction mixture was stirred at 95-100° C. for 22 hours. The DMF is removed and the residue was extracted with 800 mL dichloromethane. The organic phase was washed with 1N NaOH (2×500 mL), dried over MgSO₄ and evaporated to a brown solid of O-(2-nitro-4-chlorophenyl)salicylaldehyde (48.5 g, 83.9%), m.p. 82-83° C.,

[0219]¹H NMR (300 MHz, CDCl₃), δ 6.88 (d, 1H, J=8.1 Hz), 7.06 (d, 1H, J=9.0 Hz,), 7.31 (t, 1H, J=7.5 Hz), 7.54 (qd, 2H, J=1.2 Hz, J=2.4 Hz), 7.97 (dd, 1H, J=1.8 Hz, J=7.8 Hz), 8.04 (d, 1H, J=2.4 Hz), 10.45(d, 1H, J=0.9 Hz, —CHO).

[0220] (b) To a stirred solution of 48.5 g of O-(2-nitro-4-chlorophenyl)salicylaldehyde in 200 mL of acetone at room temperature was added 180 mL of chromic acid reagent (100 g Na₂Cr₂O₇, 153 g of concentrated H₂SO, and sufficient H₂O to make 500 ml total volume) over a period of 15 min. The solution was kept at 50° C. by cooling during the addition. After the addition was complete, the mixture was stirred for 20 hours. The acetone was removed, the residue was added into a saturated Na₂CO₃ solution. After filtration, the filtrate was neutralized with concentrated HCl to provide a yellow solid of O-(2-nitro-4-chlorophenyl)salicylic acid, 33.74 g (65.8%), mp 155-160°, ¹H NMR (300 MHz, CDCl3), δ 6.887 (d, 1H, J=9.0 Hz), 7.04 (dd, 1H, J=0.9 Hz, J=8.1 Hz), 7.36 (t, 1H, J=8.1 Hz), 7.48 (dd, 1H, J=2.7 Hz, J=9.0 Hz), 7.60 (dd, 1H, J=1.5 Hz, J=8.1 Hz), 8.01(d, 1H, J=2.4 Hz), 8.15 (dd, 1H, J=1.8 Hz, J=8.1 Hz).

[0221] (c) A solution of 33.74 g of O-(2-nitro-4-chlorophenyl)salicylic acid in 150 mL of methanol was hydrogenated over Raney nickel (6.8 g) at room temperature and 30 psi pressure with stirring for 20 hours. The crude amino acid obtained on evaporation of the methanol was refluxed in 150 mL of xylene for 20 hours with continuous removal of water. The xylene solution was cooled and the xylene was removed, the residue was washed with THF, filtered and dried to provide 8-chloro-10H-dibenzo[b,f][1,4]oxazepin-11-one as gray solid (13.3 g, 40%), mp 260-261°. 1H NMR (300 MHz, DMSO-d⁶), δ 7.15-7.2 (m, 2H), 7.3-7.4 (m, 3H), 7.64 (ddd, 1H, J=1.9, 7.8 and 8.4 Hz), 7.78 (dd, 1H, J=1.5 and 7.7 Hz), 10.589 (s, 1H, —NH).

Example 19 8-Fluoro-10H-dibenzo[b,f][1,4]oxazepin-11-one (Formula 2, X=O, R¹=F)

[0222] This was obtained following the procedure of Example 18 using 2,5-difluoronitrobenzene in place of 2,5-dichloronitrobenzene in step (a). The intermediate O-(2-nitro-4-fluorophenyl)salicylaldehyde had a ¹H NMR (300 MHz, CDCl₃) □ 6.82 (d, 1H, J=8.4 Hz), 7.15-7.40 (m, 3H), 7.54 (ddd, 1H, J=1.9, 7.6 and 8.1 Hz), 7.81 (dd, 1H, 2.3 and 7.6 Hz), 7.97 (dd, 1H, J=1.7 and 8.8 Hz), 10.50 (d, 1H, J=0.9 Hz, —CHO). The intermediate O-(2-nitro-4-fluorophenyl)salicylic acid had a ¹H NMR (300 MHz, CDCl₃) □ 6.95-7.05 (m, 2H), 7.25-7.35 (m, 2H), 7.60 (ddd, 1H, J=1.9, 7.6 and 8.1 Hz), 7.79 (dd, 1H, 2.7 and 7.6 Hz), 8.16 (dd, 1H, J=1.5 and 8.6 Hz). 8-Fluoro-10H-dibenzo[b,f][1,4]oxazepin-11-one had a mp 228-229° C. and ¹H NMR (300 MHz, DMSO-d⁶), δ 6.95-7.05 (m, 2H), 7.31-7.42 (m, 3H), 7.60 (ddd, 1H, J=1.8, 7.6 and 8.12 Hz), 7.79 (dd, 1H, J -1.3 Hz and 7.7 Hz), 10.64 (s, 1H, —NH).

Example 20 8-Chloro-10H-dibenzo[b,f][1,4]thiazepin-11-one (Formula 2, X=S, R¹=Cl)

[0223] (a) Methyl thiosalicylate (5.0 g, 0.0297 mol ) was dissolved in a solution of sodium hydroxide 1.18 g (0.030 mol) in water (2.5 mL) and methanol (60 mL). To the resulting red solution was added 6.9 g (0.036 mol) of 2,5-dichloronitrobenzene dissolved in methanol (20 mL). The mixture was refluxed for 23 h. The reaction mixture was cooled to room temperature, partitioned between equal parts diethyl ether and water, and shaken vigorously. The aqueous layer was drawn from the funnel, and the resulting organic phase was dried over MgSO₄, filtered, and concentrated in vacuo to provide yellow crystals of methyl S-(2-nitro-4-chloromethylphenyl)thiosalicylate (9.13 g, 95%), ¹H NMR (300 MHz, CDCl₃), δ 3.822 (s, 3H, —OCH₃), 6.95 (d, 1H), 7.26 (s, 1H), 7.49 (dd, 1H, J=1.5 Hz), 7.45-7.47 (m, 2H), 7.90 (dd, 1H), 8.12 (d, 1H).

[0224] (b) A solution of 9.0 g (27.8 mmol) of methyl S-(2-nitro-4-chloromethylphenyl)thiosalicylate in 100 mL of methanol was hydrogenated over Raney nickel (1.12 g) at room temperature and 30 psi pressure with stirring for 17 hours. The residue obtained on evaporation of the methanol was dissolved in chloroform, filtered, dried over MgSO₄, filtered, and concentrated in vacuo to provide methyl S-(2-amino-4-chloromethylphenyl)thiosalicylate as a white solid (8.16 g, 55.6%), ¹H NMR (300 MHz, CDCl₃) δ 4.00 (s, 3H, —OCH₃), 4.40 (s, 2H, —NH₂), 6.77 (dd, 1H, J=1.2 Hz), 6.79 (dd, 1H, J=2.1 Hz), 6.84 (dd, 1H, J=2.4 Hz), 7.15-7.20 (m, 1H), 7.28-7.34 (m, 1H), 7.40 (d, 1H, J=8.1 Hz), 8.006 (dd, 1H, J=1.5 Hz).

[0225] (c) 8.16 g Methyl S-(2-amino-4-chloromethylphenyl)thiosalicylate was dissolved in THF (50 mL) and methanol (50 mL), and treated with SN sodium hydroxide solution (20 mL) with stirring at room temperature for 17 h. The reaction mixture was concentrated in vacuo, diluted with water, and acidified to pH 1-2 with 6N hydrochloric acid. The resulting suspension was filtered, and recrystallized from n-heptane to provide S-(2-amino-4-chloromethylphenyl)thiosalicylic acid as a light gray solid, ¹H NMR (300 MHz, CDCl₃), δ 6.77 (dd, 1H, J=2.7 Hz, J=2.1 Hz), 6.83 (d, 1H, J=2.1 Hz), 7.18 (t, 1H), 7.367 (s, 1H), 7.32 (t, 1H), 7.38 (d, 1H, J=8.4 Hz), 8.13 (d, 1H, J=1.8 Hz).

[0226] (d) S-(2-Amino-4-chloromethylphenyl)thiosalicylic acid was refluxed in 150 mL of xylene for 21 h with continuous removal of H₂O. The xylene was removed, the residue was washed with 95% ethanol, filtered and dried to provide 8-chloro-10H-dibenzo[b,f][1,4]thiazepin-11-one as a white solid of mp 163-165° C., ¹H NMR (300 MHz, DMSO-d⁶), δ 7.22 (dd, 1H, J=2.4 and 8.5 Hz), 7.28 (d, 1H, J=2.4 Hz), 7.44-7.53 (m, 3H), 7.58 (d, 1H, J=8.4 Hz), 7.68 (m, 1H), 10.80 (s, 1H).

Example 21 Binding Affinity and K_(off)

[0227] A desirable feature of a compound of the present invention is a low affinity and a fast K_(off) (as predicted by low affinity). As mentioned hereinabove a preferred affinity (K_(i)) is above about 40 nM. Compounds of the invention have been tested for their affinity using the methods described in Seeman et al. (1993) using ³H-raclopride as ligand. The results are provided in Table 2. TABLE 2 Summary of Binding Data Example Number K_(i) (nM)  1 258  2 414  3 n/a  4 215  5 250  6  42  7 108  8  23  9 150 10  28 11 n/a 12  63 13  88 14 n/a 15  58 16 n/a K_(i) values of various compounds for comparison Isoloxapine 20 Loxapine 9.8 Isoclozapine 15 Clozapine 76

Example 22 D₂ Receptor Occupancy and Catalepsy

[0228] To document the fact that the compounds cross the blood brain barrier, occupancy at the dopamine D₂ receptors using in-vivo occupancy measures was examined in rats. The test compound was injected subcutaneously followed 30 minutes later by an intravenous injection of ³H-raclopride. The animals were sacrificed 1 hour after drug administration. In animals combining occupancy and catalepsy, rats were tested for catalepsy 10 minutes before sacrifice. Animals were sacrificed by decapitation. Striata and cerebella were rapidly dissected, processed and analyzed as described by Kapur et al. (2000b) Compounds which crossed the blood brain barrier and gave predictable dose-response relationships were then tested to see if they gave catalepsy. Catalepsy is the time-honoured animal model to predict the propensity of compounds to give rise to extrapyramidal side-effects in humans. Catalepsy was measured using a grid-test by a rater blind to the treatment-assignment. The time that animals remained immobile was used as an index of catalepsy by transforming raw-scores into catalepsy scores, with a score of 1 as questionable catalepsy and scores of 2-5 reflecting severity of catalepsy (Ahlenius S et al. 1986). To validate this procedure it was first documented that haloperidol (a drug known to give rise to motor side-effects in humans) gave rise to robust catalepsy at doses above 0.25 mg/kg/sc while clozapine (a drug known not to give rise to motor side-effects in humans) did not give rise to catalepsy at doses up to 20 mg/kg/sc.

[0229] The compound of Example 6 showed a dose-dependent increase in D₂ occupancy (dose 1-40 mg/kg/sc in acidified saline; occupancy 5-81%, with an ED₅₀ of about 5 mg/kg). No animals showed any evidence of motor-side-effects with this compound. The compound of Example 7 showed a dose-dependent increase in D₂ occupancy (dose 1-40 mg/kg/sc in acidified saline; occupancy 22-75% with an ED₅₀ of 10 mg/kg). No animals showed any evidence of motor-side-effects in doses up to 40 mg/kg/sc with this compound.

Example 23 Conditioned Avoidance Response

[0230] All antipsychotics show an inhibition of the conditioned “avoidance” response (CAR) at doses which do not cause catalepsy and do not cause escape deficits. Therefore the new compounds were tested for activity in this model. For conditioned avoidance-response, rats were trained and tested in a computer assisted two-way active avoidance (shuttlebox), with an 80 dB white-noise as a conditioned stimulus, followed ten seconds later by a 0.6 mA shock as the unconditioned stimulus. Details of the procedure have been described elsewhere (Wadenberg M L et al. 2000). The tests were first validated by documenting that haloperidol (>0.05 mg/kg/sc) and clozapine (>10 mg/kg/sc) gave rise to robust inhibition of avoidance, without catalepsy or escape deficits. The compound of Example 6 showed >50% inhibition of CAR at doses of 10 mg/kg/sc. The compound of example 7 showed >50% inhibition of CAR at doses of 20 mg/kg/sc.

Example 24 FOS Immunohistochemistry

[0231] It is thought that drug-induced immediate-early-gene product FOS provides a valid marker for identifying antipsychotics that do not give rise extrapyramidal side-effects. In particular, all antipsychotics induce FOS in the nucleus accumbens regions while those likely to give rise to motor side-effects also induce FOS in the dorsolateral striatum (Robertson et al. 1994). For examining the distribution of FOS protein by the test compound, the test compound was injected into rats and two hours later, the animals were deeply anaesthetized with sodium phenobarbitol (100 mg/kg i.p.) and perfused transcardially, the brains removed and post-fixed. Immunostaining was performed on free-floating forty-micron sections with a rabbit-raised polyclonal primary anti-FOS antiserum (diluted 1:250 and incubated 48 hours at 4° C.) (4-17 aminoacids of human Fos; Oncogene Research Products, Cambridge, Mass., USA). Exposure to a biotinylated goat anti-rabbit secondary antibody (1:600, Vector Laboratories, Burlingame, Calif., USA) followed by incubation with horseradish peroxidase avidin-biotin complex (Vector Laboratories, Vector Laboratories, Burlingame, Calif., USA) was used to visualize the FOS staining. Fos-immunoreactive nuclei were counted within 400×400 μm grid at a magnification of 100×in the shell of nucleus accumbens and dorsolateral striatum. This procedure was validated by showing that both haloperidol and clozapine gave robust FOS induction in the nucleus accumbens, but only haloperidol resulted in FOS in the dorsolateral striatum. In tests for FOS protein induction, the compound of Example 6 showed robust induction of FOS protein in the nucleus accumbens, with no induction of FOS protein in the dorsolateral striatum. Index of Patents No. Patent No. Issue Date Title  1. 3,347,849 Oct. 17, 1967 5-(Basic Substituted)-Dibenzodiazepines  2. 3,367,930 Feb. 6, 1968 Process for the Preparation of Heterocyclic Compounds  3. 3,412,193 Nov. 19, 199/ 11-(4-Methyl-1-Piperazinyl)dibenz[b,f][1,4]Oxazepines or Thiazepines for Controlling Fertility  4. 3,444,169 May 13, 1969 Process for 11-Aminodibenzo[bf,][1,4]Oxazepines and Analogous Thiazepines  5. 3,539,573 Nov. 10, 1970 11-Basic Substituted Dibenzodiazepines and Dibenzothiazepines  6. 3,546,226 Dec. 8, 1970 11-Basic Substituted Dibenzoxazepines  7. 3,663,696 May 16, 1972 Treatment of Depression With 2-Chloro-11- (Piperazinyldibenz-[b,f][1,4]Oxazepines and Acid Addition Salts Thereof  8. 3,681,357 Aug. 1, 1972 2-Chloro-11-(Piperazinyl)Dibenzy[b,f][1,4]Oxazepine and Acid Addition Salts Thereof  9. 5,068,437 Nov. 26, 1991 Process for Producing 2-(P-Chlorophenoxy) Aniline 10. 5,393,752 Feb. 28, 1995 Methylpiperazinoazepine Compounds, Preparation and Use Thereof 11. 5,602,120 Feb. 11, 1997 Benzyl-Substituted Compounds Having Dopamine Receptor Affinity 12. WO Dec. 18, 1998 Methods for the Simultaneous Identification of Novel 99/31267 Biological Targets and Lead Structures for Drug Development 13. 436 297 May 31, 1967 Verfahren zur Herstellung 11-Basich substituierter [CH] Dibenz[b,f]-[1,4]oxazepine 14. 1,164,360 Nov. 30, 1967 A Process for Preparing Tricyclic Organic Compounds [GB] Index of Articles No. Author Title Citation 15. Ahlenius, Involvement of Extrapyramidal Pharmac., Biochem. & Behavior, S., et al. Motor Mechanisms in the Vol. 24, PP. 1409-1415 (986) Suppression of Locomotor (Ahlenius S et al. 1986) Activity by Antipsychotic Drugs: A Comparison Between the Effects Produced by Pre- and Post-Synaptic Inhibition of Dopaminergic Neurotransmission 16. Bartl, V., et Neurotropic and Psychotropic Collection Czech. Chem. al. Agents. LXV: 8-Chloro and 8- Community (Vol. 38), pp. 2778- Isopropyl-6- 2787 (1973) Piperazinobenzo(b)Pyridol[3,2-f] Thiepin 17. Bartl, V., et Neurotropic and Psychotropic Collection Czech. Chem. al. Agents. LXI: Derivatives of 6- Community (Vol. 38), pp. 1693- Piperazinobenzo[b]Pyridol[3,2- 1699 (1973) f]Thiepin 18. Casey, D. E. Extrapyramidal Syndromes CMS Drugs, 5 Supp., pp. 1-12 (1996) (Casey 1996) 19. Farde, L., Positron Emission Tomographic Arch. Gen. Psychiatry, Vol. 49, et al. Analysis of Central D₁ and D₂ pp. 538-544 (1992) Dopamine Receptor Occupancy in (Farde et al. 1997) Patients Treated With Classical Neuroleptics and Clozapine 20. Farde, L., Central D2-Dopamine Receptor Arch. Gen. Psychiatry, Vol. 45, et al. Occupancy in Schizophrenic pp. 71-76 (1988) Patients Treated with (Farde et al. 1997) Antipsychotic Drugs 21. Jegouzo, Comparative oxidation of loxapine Fundam. Clin. Pharmacol. Vol. 13, A., et al. and clozapine by human pp. 113-119 (1999) neutrophils (Jegouzo et al. 1999) 22. Jiler, J., et Neurotrope Und Psychotrope Collection Czech. Chem. al. Substanzen. XIX: 8- Community (Vol. 33), pp. 1831- Halogenderivate von 10-(4- 1845 (1968) Methylpiperazino)-10,11- Dihydrodibenzo(b,f)Thiepin und Verwandte Substanzen 23. Kapur, S., Does Fast Dissociation From the Am. J. Psychiatry, Vol. 158: 3, pp. et al. Dopamine D₂ Receptor Explain 360-369 (March 2001) the Action of Atypical Antipsychotics?: A New Hypothesis 24. Kapur, S., Antipsychotic agents differ in how J. Psych. & Neuroscience, Vol. 25, et al. fast they come of the dopamine D₂ No. 2, pp. 161-166 (2000) receptors. Implications for (Kapur and Seeman 2000a) atypical antipsychotic action 25. Kapur, S., Are Animal Studies of Can. J. Psychiatry, Vol. 45, pp. et al. Antipsychotics Appropriately 241-245 (2000) Dosed?: Lessons From the (Kapur et al. 2000b) Bedside to the Bench 26. Liegeois, Pyrodibenzoxazepine and J. Med. Chem. Vol. 37, pp. 519- J. F., et al. Pyridobenzothiazepine 525, 1994 Derivatives as Potential Central Nervous System Agents: Synthesis and Neurochemical Study 27. Moore, K. Interactions between Prolactin and Biology of Reproduction, Vol. 36, Dopaminergic Neurons pp. 47-58 (1987) (Moore 1987) 28. Pelz, K., et Neurotrope und Psychotrope Collection Czech. Chem. al. Substanzen. XXV: Uber die in 8- Community (Vol. 33), pp. 1895- Stellung Durch die Methyl-, Tert- 1910 (1968) Butyl-, Methoxy-, Methylthio-, und methansulfonylgruppe Substituierten 10-(4- Methylpiperazino)-10,11- Dihydrodibenzol[b,f]Thiepin- Derivate 29. Robertson, Induction Patterns of Fos-Like Jnl. Pharmacol. & Exper. Therap. G. et al. Immunoreactivity in the Forebrain Vol. 271, No. 2, pp. 1058-1066, as Predictors of Atypical 1994 Antipsychotic Activity (Robertson et al. 1994) 30. Seeman, P. Deriving the therapeutic Eur. Jnl of Pharmac., Molecular et al. concentrations for clozapine and Pharmac. Section 291, pp. 59-66, haloperidol: The apparent (1993) dissociation constant of a (Seeman 1993) neuroleptic at the dopamine D₂ receptor varies with the affinity of the competing radioligand 31. Seeman, P. Antipsychotic drugs which elicit Molecular Psych. Vol. 3, pp. 123- et al. little or no Parkinsonism bind 134, (1998) more loosely than dopamine to (Seeman and Tallerico 1998) brain D2 receptors, yet occupy high levels of these receptors 32. Seeman, P. Rapid release of Antipsychotic Am. J. Psychiatry, Vol. 156, pp. et al. Drugs From Dopamine D₂ 676-684 (1999) Receptors: An Explanation for Low Receptor Occupancy and Early Clinical Relapse Upon Withdrawal of Clozapine or Quetiapine 33. Uetrecht, J. Structural features associated with Chemico-Biological Interactions, et al. reactive metabolite formation in Vol. 104, pp. 117-129 (1997) clozapine analogues (Uetrecht et al. 1997) 34. Uetrecht, J. Reactive metabolites and Eur. Jnl Haemotology, Vol. 57, pp. et al. agranulocytosis 83-88 (1996) (Uetrecht 1996) 35. Wadenberg, Dopamine D₂ receptor occupancy Psychopharmacology, Vol. 150, M. et al. predicts catalepsy and the pp. 420-429 (2000) suppression of conditioned (Wadenberg M. L. et al. 2000) avoidance response behavior in rats

[0232] All publications, references, articles, patents and patent applications cited herein are herein incorporated by reference in their entirety to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety.

[0233] While the present invention has been described with reference to what are presently considered to be the preferred examples, it is to be understood that the invention is not limited to the disclosed examples. To the contrary, the invention is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims. 

What is claimed is:
 1. A compound of Formula I or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said Formula I is represented by:

R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano, CH₃ and CH₃O; R² is selected from the group consisting of C₂₋₅ alkyl and (CH₂)_(n)OH; X is selected from the group consisting of O and S; and n is an integer selected from 2, 3, 4 and
 5. 2. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein X is O.
 3. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein X is S.
 4. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein R¹ is C₂₋₄ alkyl.
 5. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein R¹ is selected from the group consisting of ethyl, n-propyl, isopropyl, n-butyl and (CH₂)₂OH.
 6. The compound of claim 5, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein R² is selected from the group consisting of ethyl and (CH₂)₂OH.
 7. The compound of claim 6, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein R¹ is selected from the group consisting of halo and CF₃.
 8. The compound of claim 7, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein R¹ is selected from the group consisting of F, Cl, Br and I.
 9. The compound of claim 7, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein R¹ is selected from the group consisting of C₁ and CF₃.
 10. The compound of claim 1, wherein said compound of Formula (I) is selected from the group consisting of:

(A-1)=8-Trifluoromethyl-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-2)=8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-3)=8-Trifluoromethyl-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-4)=8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-5)=8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-6)=8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-7)=8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-8)=8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-9)=8-Chloro-11 (4-ispropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-10)=8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-11)=8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-12)=8-Chloro-1-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

(A-13)=8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

(A-14)=8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

(A-15)=8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

(A-16)=8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.
 11. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value of at least 30 nM.
 12. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value from 30 nM to about 500 nM.
 13. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value of at least about 40 nM.
 14. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value from about 40 nM to about 500 nM.
 15. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value from about 40 nM to about 180 nM.
 16. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value from about 40 nM to about 80 nM.
 17. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value of at least about ½ times (K_(i) for clozapine).
 18. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound has a K_(i) value from about ½ times (K_(i) for clozapine) to about 2 times (K_(i) for clozapine).
 19. The compound of claim 1, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, wherein said compound is selected from the group consisting of:

(A-6) 8-Chloro-1-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine; and

(A-7)=8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine.
 20. A method for the treatment of psychosis, said method comprising the step of administering, to a subject in need thereof, a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, of Formula I:

R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano, CH₃ and CH₃O; R² is selected from the group consisting of C₂₋₅ alkyl and (CH₂)_(n)OH; X is selected from the group consisting of O and S; and n is an integer selected from 2, 3, 4, and
 5. 21. The method of claim 20, wherein said compound, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, of Formula I is selected from the group consisting of:

(A-1)=8-Trifluoromethyl-11 (4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-2)=8-Trifluoromethyl-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-3)=8-Trifluoromethyl-1-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-4) 8-Trifluoromethyl-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-5) 8-Trifluoromethyl-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-6)=8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-7)=8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-8)=8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-9)=8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-10)=8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-11)=8-Fluoro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]oxazepine;

(A-12)=8-Chloro-11-(4-ethylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

(A-13) 8-Chloro-11-(4-(2′-hydroxyethyl)piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine;

(A-14)=8-Chloro-11-(4-propylpiperazin-1-yl)-dibenzo[b,f][1,4]tiiazepine;

(A-15)=8-Chloro-11-(4-isopropylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine; and

(A-16)=8-Chloro-11-(4-butylpiperazin-1-yl)-dibenzo[b,f][1,4]thiazepine.
 22. A pharmaceutical composition comprising a compound of Formula I, or its pharmaceutical salt, hydrate or solvate thereof, and a pharmaceutically acceptable carrier, said Formula I represented by:

R¹ is selected from the group consisting of halo, CF₃, CF₃O, cyano, CH₃ and CH₃O; R² is selected from the group consisting of C₂₋₅ alkyl and (CH₂)_(n)OH; X is selected from the group consisting of O and S; and n is an integer selected from 2, 3, 4, and
 5. 23. The method of claim 20, wherein said administering step comprises orally administering, for the treatment of schizophrenia, said compound, or a pharmaceutically acceptable salt, hydrate, prodrug or solvate thereof, of Formula I. 